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. 2013 Jun 10;8(6):e62371. doi: 10.1371/journal.pone.0062371

Figure 1. Imaging data of VX2 tumors in rabbits.

Figure 1

(a and b) Representative gamma camera planar images of VX2 tumors (a) infected in vivo by IA and IT administration of Ad-CMV-HA-SSTR2, and (b) infected in vivo by IA infusion of Ad-CMV-HA-SSTR2 and by IT injection of control Ad-CMV-GFP (B =  bladder, S =  source of 111In for positioning). Increased 111In-octreotide uptake is seen in tumors infected with Ad-CMV-HA-SSTR2 by both routes of administration compared to infection with the control Ad-CMV-GFP. (c) 111In-octreotide biodistribution in tumors normalized to tumor weight (%ID/g) calculated with and without necrosis using imaging only (in vivo biodistribution from gamma camera and CT imaging). Uptake was higher in tumors infected with Ad-CMV-HA-SSTR2 compared to control Ad-CMV-GFP (*, p<0.01, n = 6 for IA vs GFP; p<0.01, n = 6 for IT vs GFP). No difference was seen between the IA and IT groups. (d) Contrast enhanced CT showing the small amount of necrosis within the tumors.